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Study on Adding Precisely Targeted Radiation Therapy (Stereotactic Body Radiation Therapy) to the Usual Treatment Approach (Drug Therapy) in Patients with Metastatic Breast Cancer, The AIM-B Study
Trial Status: active
This phase II trial tests whether stereotactic body radiation therapy (SBRT) works to shrink tumors in patients with breast cancer that has spread to other places in the body (metastatic). SBRT delivers extremely precise, very intense doses of radiation to tumor cells. This targeted radiation therapy kills cancer cells while sparing other, healthy cells. Using SBRT to treat one metastatic site where cancer has worsened may prevent cancer from getting worse in other metastatic sites or spreading. In addition, the combination of SBRT to a single metastatic site and usual drug therapy may be more effective than usual drug therapy alone.
Inclusion Criteria
Age 18 or older
Willing and able to provide informed consent
Metastatic breast cancer, biopsy proven
* Estrogen receptor (ER)+/HER2-, defined as > 5% ER+ staining
* HER2+ (regardless of ER status), including HER2-low and high expressors
History of at least 6 months, sustained response to systemic therapy (clinically or radiographically defined as complete or stable response without progression)
Isolated site of disease progression on fludeoxyglucose F-18 (FDG) positron emission tomography (PET) scan
Consented to 12-245
Eastern Cooperative Oncology Group (ECOG) performance status 0-1
Exclusion Criteria
Pregnancy
Serious medical comorbidity precluding radiation, including connective tissue disorders
Previous radiotherapy to the intended treatment site that precludes developing a treatment plan that respects normal tissue tolerances
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT05534438.
Locations matching your search criteria
United States
New Jersey
Basking Ridge
Memorial Sloan Kettering Basking Ridge
Status: Active
Contact: Amy Xu
Phone: 646-888-6863
Middletown
Memorial Sloan Kettering Monmouth
Status: Active
Contact: Amy Xu
Phone: 646-888-6863
Montvale
Memorial Sloan Kettering Bergen
Status: Active
Contact: Amy Xu
Phone: 646-888-6863
New York
Commack
Memorial Sloan Kettering Commack
Status: Active
Contact: Amy Xu
Phone: 646-888-6863
New York
Memorial Sloan Kettering Cancer Center
Status: Active
Contact: Amy Xu
Phone: 646-888-6863
Uniondale
Memorial Sloan Kettering Nassau
Status: Active
Contact: Amy Xu
Phone: 646-888-6863
West Harrison
Memorial Sloan Kettering Westchester
Status: Active
Contact: Amy Xu
Phone: 646-888-6863
PRIMARY OBJECTIVE:
I. To assess if stereotactic body radiation therapy (SBRT) improves 3 month progression free survival, defined as time from first SBRT treatment to disease progression or death.
SECONDARY OBJECTIVES:
I. To assess time to next line systemic therapy.
II. To assess overall survival.
III. To assess local control of irradiated lesion using positron emission tomography (PET) Response Criteria in Solid Tumors (PERCIST).
IV. To assess time to failure/progression outside of irradiated lesion.
V. To assess toxicity of SBRT.
VI. To assess long term progression free survival at 6 and 12 months.
EXPLORATORY OBJECTIVES:
I. To assess rate of circulating tumor-deoxyribonucleic acid (ctDNA) clearance 3 months following SBRT using existing data from 12-245 that corresponds with the following timepoints: screening, within one week of last radiation treatment, 3 months , 6 months and 12 months after last radiation.
II. To assess changes in ctDNA mutational profile in response to SBRT using existing data from 12-245 that corresponds with the following timepoints: screening, within one week of last radiation treatment, 3 months, 6 months and 12 months after last radiation.
OUTLINE:
Patients undergo SBRT and receive standard of care drug therapy on study. Patients undergo magnetic resonance imaging (MRI) and collection of blood samples during screening. Patients also undergo positron emission tomography (PET) throughout the trial.
After completion of study treatment, patients are followed up for 1 year.
Trial PhasePhase II
Trial Typetreatment
Lead OrganizationMemorial Sloan Kettering Cancer Center